Device Recall LP Rotate Foot System 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Ossur H / F 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

의료기기에 문제가 생겼을 경우 제조사가 이를 바로잡거나 시장에서 회수하는 조치를 말한다. 회수(Recall)는 의료기기에 결함이 있거나, 건강에 위협이 되거나, 또는 결함도 있고 건강에도 위협이 될 경우에 발생한다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Recall
  • 사례 ID
    70648
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-1288-2015
  • 사례 시작날짜
    2015-03-04
  • 사례 출판 날짜
    2015-03-17
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2015-10-28
  • 사례 출처
    USFDA
  • 사례 출처 URL
  • 비고 / 경고
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • 데이터 추가 비고
    Component, external, limb, ankle/foot - Product Code ISH
  • 원인
    The threads of the outer tube of the shock module of lp rotate are too short, resulting in insecure assembly. use of the product may cause the patient to fall with continued use, as the shock module can become loose from the foot blade.
  • 조치
    The firm's recall letter states the following instructions: Immediately examine inventory and quarantine product subject to the recall. In addition the firm asks if further distributed to identify the customers and notify them of the recall. The firm states that notification may be enhanced by providing a copy of the letter. The firm states that the recall notice needs to be passed along to all those who need to be aware. The firm also states that if customers are wearing a faulty product that they recommend them scheduling a visit to have the product replaced with a new LP Rotate that is currently available. The firm states that they can also arrange pick-up of defected products. For any questions the firm provides a customer service contact: Jamie Dutter, Senior Customer Service Representative.

Device

  • 모델명 / 제조번호(시리얼번호)
    LP Rotate, sizes 25-27 cat.1-6. Product numbers LRP062, LRF062, LRPU62, LRFU62. All from manufacturing lot number HF141022
  • 의료기기 분류등급
  • 의료기기 등급
    1
  • 이식된 장치?
    No
  • 유통
    Nationwide within the U.S. and internationally to the following foreign countries; Belgium, United Kingdom, Germany, Czech Republic, France, Israel, Poland, Spain, Australia, Japan, Mexico, Bulgaria, Canada, South Korea, Sweden, Finland,
  • 제품 설명
    LP Rotate Foot System prosthetic device for fitting lower extremity amputations. || -Low profile foot module with adjustable shock absorber and rotation || with progressive stiffening || -Build height: with male pyramid adapter 145 - 153mm (5 11/16 - 6 ) || with female pyramid adapter 153 165mm (6 - 6 1/2) || -Male pyramid adapter || -Female pyramid adapter || -Maintenance free, no lubrication required || -Maximum weight: 147kg (325lbs) || -Available in sizes 22-30
  • Manufacturer

Manufacturer

  • 제조사 주소
    Ossur H / F, Grjothals 5, Reykjavik Iceland
  • 제조사 모회사 (2017)
  • Source
    USFDA